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Mohs 显微外科手术治疗皮肤平滑肌肉瘤。

Mohs micrographic surgery for the treatment of cutaneous leiomyosarcoma.

机构信息

Skin Cancer Center, Cincinnati, Ohio 45213, USA.

出版信息

J Am Acad Dermatol. 2011 Jun;64(6):1119-22. doi: 10.1016/j.jaad.2010.11.051.

Abstract

BACKGROUND

Cutaneous leiomyosarcoma is an extremely rare, malignant mesenchymal tumor of smooth muscle origin. Although generally considered a low-grade malignancy, there may be significant local invasion and subclinical extension. Rare cases of metastasis have been reported.

OBJECTIVE

We sought to review the clinical characteristics and outcome of patients with cutaneous leiomyosarcoma treated with Mohs micrographic surgery (MMS) at our practice.

METHODS

This study is a retrospective chart review of 11 consecutive patients with cutaneous leiomyosarcoma treated with MMS from 1995 through 2009. Patient demographic data, tumor size, location, previous treatment, number of Mohs stages to obtain clearance, surgical defect size, follow-up data, and presence or absence of recurrence were compiled and tabulated.

RESULTS

The average age of our 11 patients at time of diagnosis was 54.5 years. Three lesions were located on the head/neck and trunk, respectively, and 5 lesions were located on the extremities. Average preoperative clinical lesion size was 4.69 cm(2). Average number of MMS stages required for tumor clearance was 2.4. Average size of the surgical defect was 14.95 cm(2). One lesion was recurrent at the time of presentation. All remaining tumors were untreated. Mean follow-up after diagnosis was 4.47 years. No tumors recurred after MMS.

LIMITATIONS

Our retrospective study had a small patient population, and follow-up data were less extensive for some patients.

CONCLUSIONS

These data represent the largest series in the literature of leiomyosarcoma treated with MMS, and establish that MMS is a useful modality for treating cutaneous leiomyosarcoma, a rare spindle cell malignancy that is not commonly encountered by physicians.

摘要

背景

皮肤平滑肌肉瘤是一种极其罕见的、源自平滑肌的恶性间叶组织肿瘤。尽管通常被认为是低度恶性肿瘤,但可能存在显著的局部侵袭和亚临床扩展。已有罕见转移病例的报道。

目的

我们旨在回顾在本机构中接受 Mohs 显微外科手术(MMS)治疗的皮肤平滑肌肉瘤患者的临床特征和结局。

方法

这是一项回顾性病例系列研究,纳入了 1995 年至 2009 年间接受 MMS 治疗的 11 例连续皮肤平滑肌肉瘤患者。汇总了患者的人口统计学数据、肿瘤大小、位置、既往治疗、获得完全切除所需的 MMS 阶段数、手术缺损大小、随访数据以及有无复发。

结果

诊断时,11 例患者的平均年龄为 54.5 岁。3 例病变分别位于头颈部、躯干,5 例病变位于四肢。术前临床病变平均大小为 4.69cm²。清除肿瘤所需的 MMS 阶段平均为 2.4 个。手术缺损平均大小为 14.95cm²。1 例病变在就诊时复发。其余所有肿瘤均未接受治疗。诊断后平均随访时间为 4.47 年。MMS 后无肿瘤复发。

局限性

我们的回顾性研究患者人群较小,部分患者的随访数据不够广泛。

结论

这些数据代表了文献中最大的一组接受 MMS 治疗的平滑肌肉瘤病例,证实了 MMS 是治疗皮肤平滑肌肉瘤的一种有用方法。皮肤平滑肌肉瘤是一种罕见的梭形细胞恶性肿瘤,通常不会被医生遇到。

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